Table of contents

Research Article

• Genetic disorders of collagen. (1 January, 1987)

  P Tsipouras, F Ramirez
• Noonan syndrome. (1 January, 1987)

  J E Allanson
• Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions. (1 January, 1987)

  J M Connor, L A Pirrit, J R Yates, J A Crossley, S J Imrie, J M Colgan
• The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations. (1 January, 1987)

  H Veenema, J P Geraedts, G C Beverstock, P L Pearson
• The fragile X syndrome in a large family. II. Psychological investigations. (1 January, 1987)

  H Veenema, T Veenema, J P Geraedts
• High resolution gene mapping of the human alpha globin locus. (1 January, 1987)

  R D Nicholls, J A Jonasson, J O McGee, S Patil, V V Ionasescu, D J Weatherall, D R Higgs
• DNA polymorphisms of the human alpha 1 antitrypsin gene in normal subjects and in patients with pulmonary emphysema. (1 January, 1987)

  I Hodgson, N Kalsheker
• Prenatal diagnosis of alpha 1 antitrypsin deficiency and estimates of fetal risk for disease. (1 January, 1987)

  D W Cox, T Mansfield
• Trisomy 1 in an eight cell human pre-embryo. (1 January, 1987)

  J L Watt, A A Templeton, I Messinis, L Bell, P Cunningham, R O Duncan